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Functionalization of the methyl group of 1,4-dimethyl-1,4-dihydronaphthalene-1,4-endoperoxide

Publication date1984
Abstract

The acid-catalysed cleavage of 1,4-dimethyl-1,4-dihydronaphthalene-1,4-endoperoxide gives the 4-hydroxy, methoxy, trifluoroacetoxy, formyloxy, bromo, and chloro methyl derivatives of 1-methylnaphthalene in yields of 36,38,52,76,77, and 100% respectively when water, methanol, trifluoracetic, formic, hydrobromic, or hydrochloric acids are used as reagents.

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Citation (ISO format)
JEFFORD, Charles et al. Functionalization of the methyl group of 1,4-dimethyl-1,4-dihydronaphthalene-1,4-endoperoxide. In: Journal of the Chemical Society. Chemical communications, 1984, n° 22, p. 1496–1497. doi: 10.1039/C39840001496
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ISSN of the journal0022-4936
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